Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1008584
rs1008584
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10234796
rs10234796
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1863416
Disease:
Autosomal dominant compelling helio ophthalmic outburst syndrome 		0.700 GeneticVariation GWASCAT Detection and interpretation of shared genetic influences on 42 human traits. 27182965 2016
dbSNP: rs10237317
rs10237317
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs1035010
rs1035010
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs10486866
rs10486866
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs117463770
rs117463770
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0002170
Disease:
Alopecia 		G 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs11764092
rs11764092
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0549410
Disease:
Palmar-plantar erythrodysesthesia syndrome 		0.010 GeneticVariation BEFREE A genome-wide association study did not identify any associations with PPES meeting the genome-wide significance threshold, but top variants were enriched for skin expression quantitative trait loci, including rs11764092 in AUTS2 (P = 6.45 × 10<sup>-5</sup> ). 28493546 2017
dbSNP: rs11766624
rs11766624
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0162701
Disease:
Polysomnography 		G 0.700 GeneticVariation GWASDB Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs11766624
rs11766624
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C2734068
Disease:
Arm span 		G 0.700 GeneticVariation GWASCAT Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic population. 23251661 2012
dbSNP: rs11767893
rs11767893
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs11772435
rs11772435
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11972637
rs11972637
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs12698891
rs12698891
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs13223152
rs13223152
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0021704
Disease:
Intelligence 		A 0.700 GeneticVariation GWASCAT Genome-wide association meta-analysis in 269,867 individuals identifies new genetic and functional links to intelligence. 29942086 2018
dbSNP: rs13224557
rs13224557
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs145126703
rs145126703
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0002170
Disease:
Alopecia 		T 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs1474368
rs1474368
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0002170
Disease:
Alopecia 		G 0.700 GeneticVariation GWASCAT Genetic prediction of male pattern baldness. 28196072 2017
dbSNP: rs1554401434
rs1554401434
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 		ACGCCC 0.700 CausalMutation CLINVAR
dbSNP: rs1554480537
rs1554480537
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1557970
rs1557970
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0000772
Disease:
Multiple congenital anomalies 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C4014435
Disease:
MENTAL RETARDATION, AUTOSOMAL DOMINANT 26 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183469
rs1563183469
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0175754
Disease:
Agenesis of corpus callosum 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0020505
Disease:
Hyperphagia 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1563183492
rs1563183492
Entrez Id: 26053
Gene Symbol: AUTS2
AUTS2
CUI: C0549629
Disease:
Abnormal delivery 		T 0.700 GeneticVariation CLINVAR